HCSGD entry for E2F4


1. General information

Official gene symbolE2F4
Entrez ID1874
Gene full nameE2F transcription factor 4, p107/p130-binding
Other gene symbolsE2F-4
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

color bar
This gene isn't in PPI subnetwork.

3. Gene ontology annotation

GO ID

GO term

Evidence

Category

GO:0000083Regulation of transcription involved in G1/S transition of mitotic cell cycleIEAbiological_process
GO:0000278Mitotic cell cycleIEA TASbiological_process
GO:0002064Epithelial cell developmentIEAbiological_process
GO:0003677DNA bindingIEA IMPmolecular_function
GO:0003700Sequence-specific DNA binding transcription factor activityIDA IEAmolecular_function
GO:0005515Protein bindingIPImolecular_function
GO:0005634NucleusIEAcellular_component
GO:0005654NucleoplasmTAScellular_component
GO:0005667Transcription factor complexIEAcellular_component
GO:0006351Transcription, DNA-templatedIEA TASbiological_process
GO:0006367Transcription initiation from RNA polymerase II promoterTASbiological_process
GO:0006884Cell volume homeostasisIEAbiological_process
GO:0007179Transforming growth factor beta receptor signaling pathwayTASbiological_process
GO:0008015Blood circulationIEAbiological_process
GO:0008134Transcription factor bindingIPImolecular_function
GO:0008361Regulation of cell sizeIEAbiological_process
GO:0009887Organ morphogenesisIEAbiological_process
GO:0010467Gene expressionTASbiological_process
GO:0019904Protein domain specific bindingIPImolecular_function
GO:0042127Regulation of cell proliferationIEAbiological_process
GO:0042384Cilium assemblyIEAbiological_process
GO:0045944Positive regulation of transcription from RNA polymerase II promoterTASbiological_process
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4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.40500865470.55308243230.99999024731.0000000000

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Up0.0254057936
GSE13712_SHEARUp0.0524551712
GSE13712_STATICDown-0.0827385160
GSE19018Down-0.2587117303
GSE19899_A1Down-0.0664535865
GSE19899_A2Up0.2137525496
PubMed_21979375_A1Up1.0657679139
PubMed_21979375_A2Up0.4512782499
GSE35957Up0.0957061460
GSE36640Down-0.0998823989
GSE54402Up0.3010681317
GSE9593Down-0.0036439961
GSE43922Up0.1905066966
GSE24585Down-0.5388511915
GSE37065Down-0.0777073044
GSE28863_A1Down-0.0622204789
GSE28863_A2Up0.1638158551
GSE28863_A3Down-0.4692665345
GSE28863_A4Up0.0322407242
GSE48662Up0.0845428863

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

    • mirTarBase

MiRNA_name

mirBase ID

miRTarBase ID

Experiment

Support type

References (Pubmed ID)

hsa-miR-124-3pMIMAT0000422MIRT022270MicroarrayFunctional MTI (Weak)18668037
hsa-miR-615-3pMIMAT0003283MIRT039886CLASHFunctional MTI (Weak)23622248
hsa-miR-23b-3pMIMAT0000418MIRT046375CLASHFunctional MTI (Weak)23622248
hsa-miR-197-3pMIMAT0000227MIRT048137CLASHFunctional MTI (Weak)23622248
hsa-miR-98-5pMIMAT0000096MIRT048712CLASHFunctional MTI (Weak)23622248
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    • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 2 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

22002537Recruitment of PML to the TBX2 promoter is dependent on a functional p130/E2F4 repressor complex ultimately implementing a transcriptionally inactive chromatin environment at the TBX2 promoter
10585280Here we present evidence that activation of a cAMP pathway correlates with multiple cellular changes in these cells: (1) increased expression of the transcription factor microphthalmia; (2) increased melanogenesis; (3) increased association of the cyclin-dependent kinase inhibitors (CDK-Is) p27(KIP1) and p16(INK4) with CDK2 and CDK4, respectively; (4) failure to phosphorylate the retinoblastoma protein (pRB); (5) decreased expression of E2F1, E2F2, and E2F4 proteins; (6) loss of E2F DNA-binding activity; and (7) phenotypic changes characteristic of senescent cells
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